Abstract |
We examined the roles of a chemotherapeutic reagent in both inducing apoptosis and conferring acquired tumor immunity using mouse syngeneic tumor transplantation models. A chemotherapeutic reagent, cis-diamminedichloroplatinum (II), effectively induced apoptosis in Colon-26 cells originating from a BALB/c mouse. Three intradermal inoculations of cis-diamminedichloroplatinum (II)-treated Colon-26 cells conferred tumor immunity against viable Colon-26 cells in BALB/c mice but not in athymic BALB/c mice. The acquired immunity was Colon-26 cell specific and was adoptively transferable with splenic cells. We next examined the involvement of the cross-linked ribosomal protein S19 dimer (RP S19), which is released during apoptosis, in the acquisition of tumor immunity. A Colon-26 transformant that produces a Gln137Asn-mutant RP S19 prevents the formation of a functional RP S19 dimer. Acquired tumor immunity was significantly reduced when the transformant was used in combination with anti-RP S19 antibodies as the vaccination source. These data suggest the importance of the RP S19 dimer in chemotherapeutic agent-induced acquired immunity.
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Authors | Keisuke Taniguchi, Hiroshi Nishiura, Yoshihiko Ota, Tetsuro Yamamoto |
Journal | Journal of immunotherapy (Hagerstown, Md. : 1997)
(J Immunother)
Vol. 34
Issue 1
Pg. 16-27
(Jan 2011)
ISSN: 1537-4513 [Electronic] United States |
PMID | 21150710
(Publication Type: Journal Article)
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Chemical References |
- Cancer Vaccines
- Ribosomal Proteins
- ribosomal protein S19
- Cisplatin
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Topics |
- Adoptive Transfer
- Animals
- Apoptosis
- Blotting, Western
- Cancer Vaccines
(immunology)
- Cell Line, Tumor
- Cisplatin
(pharmacology)
- Immunotherapy, Adoptive
- In Situ Nick-End Labeling
- Injections, Intradermal
- Mice
- Mice, Inbred BALB C
- Mice, Nude
- Mutation
- Neoplasm Transplantation
- Neoplasms, Experimental
- Protein Multimerization
- Ribosomal Proteins
(immunology)
- Signal Transduction
- Transplantation, Isogeneic
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